Dr Ann CurtisHonorary Lecturer
Email: ann.curtis@ncl.ac.uk Telephone: +44 (0) 191 241 8772 Fax: +44 (0) 191 241 8799 Address: Institute of Human Genetics
Bown N, Powell H, Curtis A, Taylor P. Incidence and clinical significance of FLT3 internal tandem duplications in acute myeloid leukaemia. .
In: Journal of Medical Genetics: British Human Genetics Conference . 2004, York, UK: BMJ Group.
Tennant S, Strain L, Curtis A. Incidence of deletion and duplication mutations in HNPCC patients in the NE of England .
In: Journal of Medical Genetics: British Human Genetics Conference . 2004, York, UK: BMJ Group.
Powell H, Archibald K, Mountford R, Lynch SA, Bates D, Curtis A. A deletion within the frataxin gene, combined with a GAA expansion mutation causes atypical Friedreich ataxia .
In: Journal of Medical Genetics: British Human Genetics Conference . 2003, York, UK: BMJ Group.
Roberts C, Bond P, Carpenter K, Cross G, Curtis A. Comparison of MLPA and an in-house quantitative fluorescent multiplex assay for BRCA1 dosage alterations .
In: Journal of Medical Genetics: British Human Genetics Conference . 2003, York, UK: BMJ Group.
Goodship J, Garcia CC, Blair HJ, Seager M, Coulthard A, Tennent S, Buddles M, Curtis A. Deficiency of synapsin I, a synaptic vesicle protein, causes epilepsy .
In: Journal of Medical Genetics: British Human Genetics Conference . 2003, York, UK: BMJ Group.
Sutton R, Lynch SA, Curtis A. Development of diagnostic strategy for analysis of the MNX1 gene in patients with Currarino syndrome .
In: Journal of Medical Genetics: British Human Genetics Conference . 2003, York, UK: BMJ Group.
Murphy P, Douglas F, Tobias E, Curtis A, Bond PM. Identification of a truncating mutation in the TES gene in a patient with familial ovarian cancer .
In: Journal of Medical Genetics: British Human Genetics Conference . 2003, York, UK: BMJ Group.
Roberts C, Ball S, Achermann J, Curtis A. Validation of a diagnostic protocol for the detection of mutations in the DAX-1 gene in X-linked adrenal hypoplasia congenita patients .
In: Journal of Medical Genetics: British Human Genetics Conference . 2003, York, UK: BMJ Group.
Barber T, Almeida M, Curtis A, Ball SG. Developemnt of a protein truncation test for the detection of DAX-1 mutations in AHC .
In: 84th Annual Meeting of the American Endocrine Societies . 2002, San Francisco, California, USA.
Fey C, Curtis ARJ, Chinnery PF, Lombes A, Morris CM, Curtis A, Burn J. Did neuroferritinopathy originate in France? .
In: European Journal of Human Genetics: European Society of Human Genetics European Human Genetics Conference in Conjuction With European Meeting on Psychosocial Aspects of Genetics . 2002, Strasbourg, France: Nature Publishing Group.
Crompton DE, Chinnery PF, Fey C, Curtis ARJ, Morris CM, Kierstan J, Burt A, Young F, Coulthard A, Curtis A, Ince PG, Bates D, Jackson MJ, Burn J. Neuroferritinopathy: A window on the role of iron in neurodegeneration .
In: Blood Cells, Molecules and Diseases: Meeting on Molecular and Clinical Aspects of Human Iron Metabolism . 2002, Chiemesee, Germany: Academic Press.
Chinnery PF, Brown DT, Archibald K, Curtis A, Turnbull DM. Spinocerebellar ataxia and the A3243G and A8344G mtDNA mutations .
Journal of Medical Genetics 2002, 39 (5), E22.
Fey C, Curtis ARJ, Chinnery PF, Morris CM, Ince PG, Coulthard A, Jackson MJ, Barker WA, Curtis A, Burn J. A dominant FTL mutation causes a novel and pleiotropic basal ganglia disorder that can mimic torsion-dystonia, Huntington's Disease and parkinsonism .
American Journal of Human Genetics 2001, 69 (4), 97.
Gennery AR, Dickinson AM, Brigham K, Barge D, Spickett GP, Curtis A, Spencer V, Jackson A, Carter V, Palmer P, Flood TJ, Cant AJ, Abinun M. CAMPATH-1M T-cell depleted BMT for SCID: long-term follow-up of 19 children treated 1987-98 in a single center .
Cytotherapy 2001, 3 (3), 221-232.
Gennery AR, Dickinson AM, Brigham K, Barge D, Spickett GP, Curtis A, Spencer V, Jackson A, Cavanagh G, Carter V, Palmer P, Flood TJ, Cant AJ, Abinun M. CAMPATH-1M T-cell depleted BMT for SCID: Long-term follow-up of 19 children treated 1987-98 in a single center .
Cytotherapy 2001, 3 (3), 221-232.
Curtis A, Cliff S, McCarthy E, Jackson A, Lindsay S, Curtis A. Identification of RS6PKA3 gene mutations in patients with Coffin Lowry syndrome .
In: Journal of Medical Genetics . 2001, BMJ Group.
Curtis A, Fey C, Morris CM, Ince PG, Bindoff LA, Jackson MJ, Coulthard A, Curtis A, Burn J. Mutation in ferritin light chain causes dominant adult onset basal ganglia disease .
In: Journal of Medical Genetics . 2001, BMJ Group.
Curtis ARJ, Fey C, Morris CM, Bindoff LA, Ince PG, Chinnery PF, Coulthard A, Jackson MJ, Jackson AP, McHale DP, Hay D, Barker WA, Markham AF, Bates D, Curtis A, Burn J. Mutation in ferritin light chain causes dominant adult onset neurodegeneration .
Nature Genetics 2001, 28 (4), 350-354.
Curtis ARJ, Fey C, Morris CM, Bindoff LA, Ince PG, Chinnery PF, Coulthard A, Jackson MJ, Jackson AP, McHale DP, Hay D, Barker WA, Markham AF, Bates D, Curtis A, Burn J. Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease .
Nature Genetics 2001, 28 (4), 350-354.
Burn J, Curtis AR, Bindoff L, Ince P, Coulthard A, Jackson A, Jackson M, Fey C, Hay D, Shepherd D, Bates D, Curtis A. A novel autosomal dominant basal ganglia degeneration with cavitation on 19q can mimic Parkinson's disease and Huntington's disease .
American Journal of Human Genetics 2000, 67 (4), 371-371.
Clarke MP, Barker MD, Langton KP, Curtis A, Goodship JA, Bond PM, Mitchell KA, McKie N. A novel TIMP-3 mutation reveals a common molecular phenotype in Sorsby's fundus dystrophy .
In: INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE . 2000.
Langton KP, McKie N, Curtis A, Goodship JA, Bond PM, Barker MD, Clarke M. A novel tissue inhibitor of metalloproteinases-3 mutation reveals a common molecular phenotype in Sorsby's fundus dystrophy .
Journal of Biological Chemistry 2000, 275 (35), 27027-27031.
Craggs A, West SP, Curtis A, Welfare M, Hudson M, Donaldson PT, Mansfield JC. Absence of a genetic association between IL-1RN and ulcerative colitis in multiple populations from NE England .
In: GUT . 2000.
Fidalgo P, Almeida MR, West S, Gaspar C, Maia L, Wijnen J, Albuquerque C, Curtis A, Cravo M, Fodde R, Leitao CN, Burn J. Detection of mutations in mismatch repair genes in Portuguese families with hereditary non-polyposis colorectal cancer (HNPCC) by a multi-method approach .
European Journal of Human Genetics 2000, 8 (1), 49-53.
Pinkett R, Spencer V, Curtis A, Hamzehloei T, Cross I, Burn J, Douglas F, West S, Chapman P, Gunn A. Genetic testing for familiar adenomatous polyposis coli (FAP) in Newcastle: eight years on .
In: JOURNAL OF MEDICAL GENETICS . 2000.
Creighton JE, Roberts C, Pinkett R, Lyall R, Wilson DI, Curtis A, Charnley RM. Idiopathic chronic pancreatitis is associated with mutations in the cationic trypsinogen and cystic fibrosis transmembrane conductance regulator genes .
In: GUT . 2000.
Mickleburgh I, Buddles M, West SP, Mathers JC, Curtis A. Interaction of selected food constituents with APC function in enterocytes .
In: JOURNAL OF MEDICAL GENETICS . 2000.
Creighton JE, Lyall R, Wilson DI, Curtis A, Charnley RM. Mutations of the cationic trypsinogen gene in patients with hereditary pancreatitis .
British Journal of Surgery 2000, 87 (2), 170-175.
